反应详情

In a 200-ml two-necked flask were charged 4.0 g (17.1 mmol) of 2-i-propyl-4-phenylindene, 42.3 mg (0.445 mmol) of copper cyanide, and 40 ml of diethyl ether. To the mixture was added at -78° C. 11.8 ml of 1.62 M hexane solution of n-butyllithium and the mixture was stirred at room temperature for 2 hours. Subsequently, 4.2 g (18.8 mmol) of dimethyl(2-methylindenyl)silyl chloride was added at -78° C. and the mixture was stirred at room temperature for 12 hours. After addition of aqueous ammonium chloride solution to the reaction mixture, the organic layer was washed with saturated saline and dried over sodium sulfate. The sodium sulfate was removed by filtration and the organic solvent was distilled off under reduced pressure. The residue was purified by column chromatography (silica gel, development solvent: hexane methylene chloride=9:1) to obtain 7.22 g (16.8 mmol, yield: 95%) of a pale yellow oil. The product was confirmed to be a mixture of two isomers by 1H-NMR.

1. additionTo the mixture was added at -78° C
2. washthe organic layer was washed with saturated saline
3. dry with materialdried over sodium sulfate
4. customThe sodium sulfate was removed by filtration
5. distillationthe organic solvent was distilled off under reduced pressure
6. customThe residue was purified by column chromatography (silica gel, development solvent: hexane methylene chloride=9:1)